Product NDC: | 41167-3301 |
Proprietary Name: | Bullfrog Surfer |
Non Proprietary Name: | Octinoxate and Octocrylene and Oxybenzone |
Active Ingredient(s): | .075; .1; .03 g/mL; g/mL; g/mL & nbsp; Octinoxate and Octocrylene and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41167-3301 |
Labeler Name: | Chattem, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19890101 |
Package NDC: | 41167-3301-7 |
Package Description: | 147 mL in 1 BOTTLE (41167-3301-7) |
NDC Code | 41167-3301-7 |
Proprietary Name | Bullfrog Surfer |
Package Description | 147 mL in 1 BOTTLE (41167-3301-7) |
Product NDC | 41167-3301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Octocrylene and Oxybenzone |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 19890101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chattem, Inc. |
Substance Name | OCTINOXATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | .075; .1; .03 |
Strength Unit | g/mL; g/mL; g/mL |
Pharmaceutical Classes |